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CBLL1P1 CBLL1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100128122, updated on 10-Oct-2023

Summary

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Official Symbol
CBLL1P1provided by HGNC
Official Full Name
CBLL1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:55074
See related
AllianceGenome:HGNC:55074
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See CBLL1P1 in Genome Data Viewer
Location:
Xq24
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (121025279..121026107, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (119325138..119325966, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (120159133..120159961, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene cancer/testis antigen family 47 member A2 Neighboring gene cancer/testis antigen family 47 member A1 Neighboring gene uncharacterized LOC105373328 Neighboring gene glutamate dehydrogenase 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29907 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:120331053-120332252 Neighboring gene heat shock protein family A (Hsp70) member 8 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • Cbl proto-oncogene like 1 pseudogene
  • Cbl proto-oncogene, E3 ubiquitin protein ligase-like 1 pseudogene

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_022634.1 

    Range
    101..929
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    121025279..121026107 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160027.1 Reference GRCh38.p14 PATCHES

    Range
    344682..345510 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    119325138..119325966 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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